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Metastasis-Directed Therapy: New Standard or Too Early to Change Paradigm? Publisher



Klemm J1, 2 ; Rajwa P2, 3 ; Miszczyk M4 ; Bronimann S2, 5 ; Laukhtina E2, 6 ; Tsuboi I2, 7 ; Matsukawa A2, 8 ; Parizi MK2, 9 ; Karakiewicz PI10 ; Shariat SF2, 11, 12, 13, 14, 15
Authors
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Authors Affiliations
  1. 1. Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
  2. 2. Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria
  3. 3. Department of Urology, Medical University of Silesia, Zabrze, Poland
  4. 4. 3rd Radiotherapy and Chemotherapy Department, M. Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland
  5. 5. Department of Urology, The James Buchanan Brady Urological Institute, The Johns Hopkins University School of Medicine, Baltimore, MD, United States
  6. 6. Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russian Federation
  7. 7. Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan
  8. 8. Department of Urology, Jikei University School of Medicine, Tokyo, Japan
  9. 9. Department of Urology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran
  10. 10. Cancer Prognostics and Health Outcomes Unit, University of Montreal Health Centre, Montreal, Canada
  11. 11. Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, Jordan
  12. 12. Karl Landsteiner Institute of Urology and Andrology, Vienna, Austria
  13. 13. Department of Urology, Weill Cornell Medical College, New York, NY, United States
  14. 14. Department of Urology, University of Texas Southwestern, Dallas, TX, United States
  15. 15. Department of Urology, Second Faculty of Medicine, Charles University, Prague, Czech Republic

Source: Memo - Magazine of European Medical Oncology Published:2024


Abstract

Metastasis-directed therapy (MDT) is an emerging treatment strategy for patients with oligometastatic prostate cancer (PCa), particularly for oligorecurrent disease. This review aims to summarize findings from several prospective trials in the setting of oligorecurrent PCa. We found that MDT is feasible, has high tolerability, and is effective in terms of local control of treated lesions and of deferring disease progression in well-selected patients. Selecting patients for MDT requires thoughtful consideration of factors such as the castration status, the number of detected metastases, and the imaging modality used for metastasis detection. Notably, the studies included in this review varied in terms of these factors, complicating the comparability of their results. Despite the existence of several prospective clinical trials in the field, there is an absence of high-level evidence attributable to the lack of phase 3 clinical trials. As a result, current guidelines recommend the administration of MDT exclusively within the context of clinical trials. Despite this, retrospective series indicate that MDT is already frequently utilized outside of clinical trials. © The Author(s) 2023.